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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911438Generated: November 2, 2026

Hydrochloric Acid → 2,2,2-Trifluoro-1-(pyridin-2-yl)ethan-1-ol

https://huagongshe.com/reaction/911438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2-PyridinecarboxaldehydeHCID 14273—
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
CatalystTetrahydrofuranHCID 8028—
SolventTetrahydrofuranHCID 8028—
SolventSodium HydroxideHCID 14798—
Product2,2,2-Trifluoro-1-(pyridin-2-yl)ethan-1-olHCID 1374292693.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 2-pyridine carboxaldehyde (2.09 g, 19.5 mmol) and (trifluoromethyl)trimethylsilane (3.33 g, 23.4 mmol) in THF (30 mL) at 0° C. add 1M tetrabutylammonium fluoride in THF (956 μl, 0.956 mmol). Continue stirring for 30 min at 0° C. and then at ambient temperature for 2 h. Add 1M aqueous HCl (20 mL) and stir 2 h at ambient temperature. Dilute with aqueous 1M aqueous NaOH to pH 8, extract the mixture three times with EtOAc, dry over anhydrous Na2SO4, and concentrate in vacuo. Purify by chromatography eluting with hexane/EtOAc (8:2) to give the desired intermediate as a yellow oil (3.22 g, 93%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022062B2
Source datasetuspto-grants-2011_09
ORD IDord-4b60bb46f1114f92af2633b332d1220f
Source noteuspto-grants-2011_09